rdf:type |
|
lifeskim:mentions |
umls-concept:C0007634,
umls-concept:C0017262,
umls-concept:C0030685,
umls-concept:C0033554,
umls-concept:C0038435,
umls-concept:C0185117,
umls-concept:C0241938,
umls-concept:C0387583,
umls-concept:C0391871,
umls-concept:C0442805,
umls-concept:C0680255,
umls-concept:C1283071,
umls-concept:C1423524,
umls-concept:C1963578,
umls-concept:C2911684
|
pubmed:issue |
32
|
pubmed:dateCreated |
1997-9-5
|
pubmed:abstractText |
This report examines the effect of cell volume expansion on cyclooxygenase-2 (COX-2) mRNA expression, COX-2 protein expression, and prostaglandin E2 release from human amnion-derived WISH cells. Earle's balanced salts solution (EBSS) with limited NaCl concentration was utilized as the induction medium. COX-2 mRNA was elevated 6-fold in cells incubated for 1 h in hypotonic EBSS. COX-2 mRNA expression was not increased when raffinose or sucrose were used to reconstitute low NaCl. Actinomycin D blocked COX-2 mRNA increase by hypotonic stress, while cycloheximide enhanced COX-2 mRNA expression. COX-2 mRNA and protein concentrations increased as a function of decreasing media osmolarity and incubation time in hypotonic EBSS. Hypotonic EBSS induced a 3-fold increase in prostaglandin E2 release. WISH cells transiently transfected with a luciferase expression vector driven by the human COX-2 promoter for the COX-2 gene show a 3-fold increase in luciferase activity when incubated in hypotonic EBSS. COX-2 mRNA levels in primary human amnion cells were also increased by hypotonic stress. This study suggests that amnion cell COX-2 gene expression is regulated by cell volume expansion and/or increased plasma membrane tension.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cycloheximide,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclooxygenase 2,
http://linkedlifedata.com/resource/pubmed/chemical/Dactinomycin,
http://linkedlifedata.com/resource/pubmed/chemical/Dinoprostone,
http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/PTGS2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Prostaglandin-Endoperoxide Synthases,
http://linkedlifedata.com/resource/pubmed/chemical/Prostaglandins,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Synthesis Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
|
pubmed:issn |
0021-9258
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:day |
8
|
pubmed:volume |
272
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
20118-24
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:9242685-Amnion,
pubmed-meshheading:9242685-Cells, Cultured,
pubmed-meshheading:9242685-Cycloheximide,
pubmed-meshheading:9242685-Cyclooxygenase 2,
pubmed-meshheading:9242685-Dactinomycin,
pubmed-meshheading:9242685-Dinoprostone,
pubmed-meshheading:9242685-Humans,
pubmed-meshheading:9242685-Isoenzymes,
pubmed-meshheading:9242685-Membrane Proteins,
pubmed-meshheading:9242685-Osmotic Pressure,
pubmed-meshheading:9242685-Promoter Regions, Genetic,
pubmed-meshheading:9242685-Prostaglandin-Endoperoxide Synthases,
pubmed-meshheading:9242685-Prostaglandins,
pubmed-meshheading:9242685-Protein Synthesis Inhibitors,
pubmed-meshheading:9242685-RNA, Messenger
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pubmed:year |
1997
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pubmed:articleTitle |
Hypotonic stress increases cyclooxygenase-2 expression and prostaglandin release from amnion-derived WISH cells.
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pubmed:affiliation |
Labor Focus Research Group, Case Western Reserve University School of Medicine, MetroHealth Medical Center, Cleveland, Ohio 44109, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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